Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.23532378_23536675delCA913190465NPC1c.3243_3755-94del
c.2321_2833-94del
c.3294_3805+977del
c.3294_3806-94del
c.3243_3754+977del
c.2829_3340+977del
ClinVar
18g.23535624C>ACA401791449NPC1c.3322G>T (p.Ala1108Ser)
c.77G>T
n.77G>T
c.2400G>T
c.3373G>T (p.Ala1125Ser)
c.2908G>T (p.Ala970Ser)
18g.23535624C=CA2290163919NPC1c.3322G= (p.Ala1108=)
c.77G=
n.77G=
c.2400G=
c.3373G= (p.Ala1125=)
c.2908G= (p.Ala970=)
18g.23535624C>GCA401791448NPC1c.3322G>C (p.Ala1108Pro)
c.77G>C
n.77G>C
c.2400G>C
c.3373G>C (p.Ala1125Pro)
c.2908G>C (p.Ala970Pro)
18g.23535624C>TCA8912798NPC1c.3322G>A (p.Ala1108Thr)
c.77G>A
n.77G>A
c.2400G>A
c.3373G>A (p.Ala1125Thr)
c.2908G>A (p.Ala970Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.23535624dupCA2580095546NPC1c.3322dup (p.Ala1108GlyfsTer13)
c.77dup
n.77dup
c.2400dup
c.3373dup (p.Ala1125GlyfsTer13)
c.2908dup (p.Ala970GlyfsTer13)
ClinVar dbSNP gnomAD v4
18g.23535625G>ACA8912800NPC1c.3321C>T (p.Gly1107=)
c.76C>T
n.76C>T
c.2399C>T
c.3372C>T (p.Gly1124=)
c.2907C>T (p.Gly969=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
18g.23535625G>CCA503521738NPC1c.3321C>G (p.Gly1107=)
c.76C>G
n.76C>G
c.2399C>G
c.3372C>G (p.Gly1124=)
c.2907C>G (p.Gly969=)
18g.23535625G=CA2290163920NPC1c.3321C= (p.Gly1107=)
c.76C=
n.76C=
c.2399C=
c.3372C= (p.Gly1124=)
c.2907C= (p.Gly969=)
18g.23535625G>TCA8912799NPC1c.3321C>A (p.Gly1107=)
c.76C>A
n.76C>A
c.2399C>A
c.3372C>A (p.Gly1124=)
c.2907C>A (p.Gly969=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.23535626C>ACA401791450NPC1c.3320G>T (p.Gly1107Val)
c.75G>T
n.75G>T
c.2398G>T
c.3371G>T (p.Gly1124Val)
c.2906G>T (p.Gly969Val)
18g.23535626C>GCA401791451NPC1c.3320G>C (p.Gly1107Ala)
c.75G>C
n.75G>C
c.2398G>C
c.3371G>C (p.Gly1124Ala)
c.2906G>C (p.Gly969Ala)
18g.23535626C>TCA401791452NPC1c.3320G>A (p.Gly1107Asp)
c.75G>A
n.75G>A
c.2398G>A
c.3371G>A (p.Gly1124Asp)
c.2906G>A (p.Gly969Asp)
18g.23535628dupCA2573155192NPC1c.3320dup (p.Ala1108ArgfsTer13)
c.75dup
n.75dup
c.2398dup
c.3371dup (p.Ala1125ArgfsTer13)
c.2906dup (p.Ala970ArgfsTer13)
ClinVar dbSNP
18g.23535627C>ACA401791453NPC1c.3319G>T (p.Gly1107Cys)
c.74G>T
n.74G>T
c.2397G>T
c.3370G>T (p.Gly1124Cys)
c.2905G>T (p.Gly969Cys)
18g.23535627C>GCA401791454NPC1c.3319G>C (p.Gly1107Arg)
c.74G>C
n.74G>C
c.2397G>C
c.3370G>C (p.Gly1124Arg)
c.2905G>C (p.Gly969Arg)
18g.23535627C>TCA401791455NPC1c.3319G>A (p.Gly1107Ser)
c.74G>A
n.74G>A
c.2397G>A
c.3370G>A (p.Gly1124Ser)
c.2905G>A (p.Gly969Ser)
gnomAD v4
18g.23535628C>ACA503521739NPC1c.3318G>T (p.Leu1106=)
c.73G>T
n.73G>T
c.2396G>T
c.3369G>T (p.Leu1123=)
c.2904G>T (p.Leu968=)
18g.23535628C=CA2290163921NPC1c.3318G= (p.Leu1106=)
c.73G=
n.73G=
c.2396G=
c.3369G= (p.Leu1123=)
c.2904G= (p.Leu968=)
18g.23535628C>GCA503521740NPC1c.3318G>C (p.Leu1106=)
c.73G>C
n.73G>C
c.2396G>C
c.3369G>C (p.Leu1123=)
c.2904G>C (p.Leu968=)
18g.23535628C>TCA503521741NPC1c.3318G>A (p.Leu1106=)
c.73G>A
n.73G>A
c.2396G>A
c.3369G>A (p.Leu1123=)
c.2904G>A (p.Leu968=)
ClinVar dbSNP gnomAD v2 gnomAD v4
18g.23535629A>CCA401791456NPC1c.3317T>G (p.Leu1106Arg)
c.72T>G
n.72T>G
c.2395T>G
c.3368T>G (p.Leu1123Arg)
c.2903T>G (p.Leu968Arg)
18g.23535629A>GCA401791457NPC1c.3317T>C (p.Leu1106Pro)
c.72T>C
n.72T>C
c.2395T>C
c.3368T>C (p.Leu1123Pro)
c.2903T>C (p.Leu968Pro)
18g.23535629A>TCA401791458NPC1c.3317T>A (p.Leu1106Gln)
c.72T>A
n.72T>A
c.2395T>A
c.3368T>A (p.Leu1123Gln)
c.2903T>A (p.Leu968Gln)
18g.23535630G>ACA503521742NPC1c.3316C>T (p.Leu1106=)
c.71C>T
n.71C>T
c.2394C>T
c.3367C>T (p.Leu1123=)
c.2902C>T (p.Leu968=)
18g.23535630G>CCA401791459NPC1c.3316C>G (p.Leu1106Val)
c.71C>G
n.71C>G
c.2394C>G
c.3367C>G (p.Leu1123Val)
c.2902C>G (p.Leu968Val)
gnomAD v4
18g.23535630G>TCA401791460NPC1c.3316C>A (p.Leu1106Met)
c.71C>A
n.71C>A
c.2394C>A
c.3367C>A (p.Leu1123Met)
c.2902C>A (p.Leu968Met)
18g.23535631G>ACA503521743NPC1c.3315C>T (p.Ser1105=)
c.70C>T
n.70C>T
c.2393C>T
c.3366C>T (p.Ser1122=)
c.2901C>T (p.Ser967=)
ClinVar dbSNP gnomAD v4
18g.23535631G>CCA503521744NPC1c.3315C>G (p.Ser1105=)
c.70C>G
n.70C>G
c.2393C>G
c.3366C>G (p.Ser1122=)
c.2901C>G (p.Ser967=)
18g.23535631G>TCA503521745NPC1c.3315C>A (p.Ser1105=)
c.70C>A
n.70C>A
c.2393C>A
c.3366C>A (p.Ser1122=)
c.2901C>A (p.Ser967=)
18g.23535632G>ACA401791462NPC1c.3314C>T (p.Ser1105Phe)
c.69C>T
n.69C>T
c.2392C>T
c.3365C>T (p.Ser1122Phe)
c.2900C>T (p.Ser967Phe)
dbSNP
18g.23535632G>CCA401791463NPC1c.3314C>G (p.Ser1105Cys)
c.69C>G
n.69C>G
c.2392C>G
c.3365C>G (p.Ser1122Cys)
c.2900C>G (p.Ser967Cys)
18g.23535632G>TCA401791461NPC1c.3314C>A (p.Ser1105Tyr)
c.69C>A
n.69C>A
c.2392C>A
c.3365C>A (p.Ser1122Tyr)
c.2900C>A (p.Ser967Tyr)
ClinVar
18g.23535633A>CCA401791464NPC1c.3313T>G (p.Ser1105Ala)
c.68T>G
n.68T>G
c.2391T>G
c.3364T>G (p.Ser1122Ala)
c.2899T>G (p.Ser967Ala)
18g.23535633A>GCA401791465NPC1c.3313T>C (p.Ser1105Pro)
c.68T>C
n.68T>C
c.2391T>C
c.3364T>C (p.Ser1122Pro)
c.2899T>C (p.Ser967Pro)
18g.23535633A>TCA401791466NPC1c.3313T>A (p.Ser1105Thr)
c.68T>A
n.68T>A
c.2391T>A
c.3364T>A (p.Ser1122Thr)
c.2899T>A (p.Ser967Thr)
18g.23535633_23535635delCA2641278434NPC1c.3311_3313del (p.Val1104_Ser1105delinsAla)
c.66_68del
n.66_68del
c.2389_2391del
c.3362_3364del (p.Val1121_Ser1122delinsAla)
c.2897_2899del (p.Val966_Ser967delinsAla)
gnomAD v4
18g.23535634C>ACA503521746NPC1c.3312G>T (p.Val1104=)
c.67G>T
n.67G>T
c.2390G>T
c.3363G>T (p.Val1121=)
c.2898G>T (p.Val966=)
18g.23535634C=CA2290163922NPC1c.3312G= (p.Val1104=)
c.67G=
n.67G=
c.2390G=
c.3363G= (p.Val1121=)
c.2898G= (p.Val966=)
18g.23535634C>GCA503521747NPC1c.3312G>C (p.Val1104=)
c.67G>C
n.67G>C
c.2390G>C
c.3363G>C (p.Val1121=)
c.2898G>C (p.Val966=)
18g.23535634C>TCA8912801NPC1c.3312G>A (p.Val1104=)
c.67G>A
n.67G>A
c.2390G>A
c.3363G>A (p.Val1121=)
c.2898G>A (p.Val966=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.23535635A>CCA401791467NPC1c.3311T>G (p.Val1104Gly)
c.66T>G
n.66T>G
c.2389T>G
c.3362T>G (p.Val1121Gly)
c.2897T>G (p.Val966Gly)
18g.23535635A>GCA401791468NPC1c.3311T>C (p.Val1104Ala)
c.66T>C
n.66T>C
c.2389T>C
c.3362T>C (p.Val1121Ala)
c.2897T>C (p.Val966Ala)
18g.23535635A>TCA401791469NPC1c.3311T>A (p.Val1104Glu)
c.66T>A
n.66T>A
c.2389T>A
c.3362T>A (p.Val1121Glu)
c.2897T>A (p.Val966Glu)
18g.23535636C>ACA401791470NPC1c.3310G>T (p.Val1104Leu)
c.65G>T
n.65G>T
c.2388G>T
c.3361G>T (p.Val1121Leu)
c.2896G>T (p.Val966Leu)
18g.23535636C=CA2290163923NPC1c.3310G= (p.Val1104=)
c.65G=
n.65G=
c.2388G=
c.3361G= (p.Val1121=)
c.2896G= (p.Val966=)
18g.23535636C>GCA401791471NPC1c.3310G>C (p.Val1104Leu)
c.65G>C
n.65G>C
c.2388G>C
c.3361G>C (p.Val1121Leu)
c.2896G>C (p.Val966Leu)
18g.23535636C>TCA401791472NPC1c.3310G>A (p.Val1104Met)
c.65G>A
n.65G>A
c.2388G>A
c.3361G>A (p.Val1121Met)
c.2896G>A (p.Val966Met)
18g.23535637A=CA2290163924NPC1c.3309T= (p.Gly1103=)
c.64T=
n.64T=
c.2387T=
c.3360T= (p.Gly1120=)
c.2895T= (p.Gly965=)
18g.23535637A>CCA503521748NPC1c.3309T>G (p.Gly1103=)
c.64T>G
n.64T>G
c.2387T>G
c.3360T>G (p.Gly1120=)
c.2895T>G (p.Gly965=)

Number of alleles fetched